FDA.reportPublic FDA data

NDC 0061-1838 - Banamine-S

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
0061-1838
Package NDCs from labels
0061-1838-30
Manufacturer
Merck Sharp & Dohme Corp.
Effective date
2024-11-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Banamine ® -S (flunixin meglumine injection)Merck Sharp & Dohme Corp.2024-11-15PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0061-1838-30Banamine-S1 in 1 CARTONINJECTION13
0061-1838-30Banamine-S100 mL in 1 VIAL, MULTI-DOSEINJECTION1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0061-1838BANAMINE-S (FLUNIXIN) INJECTION [MERCK SHARP & DOHME CORP.]32 package rows20241116_653fa86f-42d3-4817-aae3-b0fb4710f8e5.zip

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.